FDA UDI Not in Commercial Distribution 🇺🇸 United States

PHENIX

DI: 00840916145200 · Model: 8178-1212F-10P · SPINAL ELEMENTS
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PHENIX
Primary DI
00840916145200
Version / Model
8178-1212F-10P
Company Name
SPINAL ELEMENTS
Labeler DUNS
004022104
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-01-13
Public Version
3
Public Version Date
2023-05-03
Public Version Status
Update
Public Device Record Key
2cdfb8be-32dd-4336-99c5-5113e89fbdd0
Distribution End Date
2022-07-21

Device Description

Phenix Trial & Rasp, 12 x 12 x 10mm Parallel

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
Yes
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
LXH Orthopedic Manual Surgical Instrument

GMDN Terms

Code Name
13180 Orthopaedic prosthesis implantation positioning instrument, reusable

Identifiers

Type ID
Primary 00840916145200